(R)-3-Amino-gamma-butyrolactone hydrochloride

Base Information

• Chemical Name: (R)-3-Amino-gamma-butyrolactone hydrochloride
• CAS No.: 117752-88-2
• Molecular Formula: C4H7NO2.ClH
• Molecular Weight: 137.565
• Hs Code.: 2932209090
• European Community (EC) Number: 868-674-6
• DSSTox Substance ID: DTXSID80693595
• Mol file: 117752-88-2.mol

Synonyms:117752-88-2;(R)-3-Amino-gamma-butyrolactone hydrochloride;(R)-3-Amino-g-butyrolactone hydrochloride;(R)-4-Aminodihydrofuran-2(3H)-one hydrochloride;(4R)-4-aminooxolan-2-one;hydrochloride;MFCD12545886;2(3H)-Furanone, 4-aminodihydro-, hydrochloride, (R)-;(4R)-4-Aminotetrahydrofuran-2-one hydrochloride;(4R)-4-AMINOOXOLAN-2-ONE HCL;(4R)-4-AMINOOXOLAN-2-ONE HYDROCHLORIDE;(R)-3-Amino-gamma-butyrolactonehydrochloride;DTXSID80693595;CS-B1346;d-3-aminobutyrolactone hydrochloride;FD1175;AKOS015849283;(R)-4-Aminotetrahydrofuran-2-one HCl;(4R)-4-amino-2-oxolanone hydrochloride;(R)-3-Amino-g-butyrolactonehydrochloride;DS-14334;EN300-7394785;(R)-4-amino-dihydrofuran-2(3H)-one hydrochloride;A803819;J-502212;(4R)-4-Aminooxolan-2-one--hydrogen chloride (1/1);(4R)-4-Aminodihydro-2(3H)-furanone hydrochloride (1:1);2(3H)-Furanone, 4-aminodihydro-, hydrochloride (1:1), (4R)-

Chemical Property of (R)-3-Amino-gamma-butyrolactone hydrochloride

Chemical Property:

• PSA: 52.32000
• LogP: 0.76290
• Storage Temp.: Inert atmosphere,Room Temperature
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 137.0243562
• Heavy Atom Count: 8
• Complexity: 91.7

Purity/Quality:

99%min ^*data from raw suppliers

(R)-3-Amino-g-butyrolactoneHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(COC1=O)N.Cl
• Isomeric SMILES: C1[C@H](COC1=O)N.Cl

Technology Process of (R)-3-Amino-gamma-butyrolactone hydrochloride

There total 1 articles about (R)-3-Amino-gamma-butyrolactone hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(S)-3-acetylamino-y-butyrolactone (754228-95-0) → (R)-β-amino-γ-butyrolactone hydrochloride (117752-88-2)

Guidance literature:

With hydrogenchloride; for 2h; Heating;

Reference yield:

Benzophenone imine (1013-88-3) + (R)-β-amino-γ-butyrolactone hydrochloride (117752-88-2) → (R)-β-(diphenylmethylene)amino-γ-butyrolactone (117752-89-3)

Guidance literature:

In dichloromethane; Yield given; Ambient temperature;

upstream raw materials:

(S)-3-acetylamino-y-butyrolactone

Downstream raw materials:

(R)-β-(diphenylmethylene)amino-γ-butyrolactone

Refernces